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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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All-In — 10 UDI-DI variants, MDR (MEDICAL PRECISION IMPLANTS, S.A.)

MD Atlas
MEDICAL PRECISION IMPLANTS, S.A.

Data from EUDAMED, last updated May 23, 2026

All-In

084357230iacmNH

10 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: MEDICAL PRECISION IMPLANTS, S.A.

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Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 084357230iacmNH
Device name: —
Device model: All-In
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Mar 19, 2026

Manufacturer & authorised representative

Manufacturer

Name: MEDICAL PRECISION IMPLANTS, S.A.
SRN: ES-MF-000008091
Country: Spain
Email: r.bosch@mpimplants.com
Phone: +34916846063

Variants by status

UDI-DI variants

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KM2TVRG4H9HFG1XM9DTPETY7

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

IACM41308435723001881
IACM41008435723001867
IACM371108435723001829
IACM51308435723001928
IACM371008435723001812
IACM51008435723001904
IACM31108435723001775
IACM31008435723001768
IACM371308435723001836
IACM4808435723001850